BEUDAMED
    16 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    NeuroNav System, NeuroSmart System

    FDA 510(k)
    FDA Class 2 ·Neurology

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694027144·2.0mm X 42mm Cannulated Headless Screw

    External Fixation

    FDA UDI
    Life Spine, Inc.·00190837023300·Medium Strut

    SN R3 Locking Shaft

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215076498·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694068727·Cannulated 2.0 x 42mm Headless Screw Sterile Qty 5

    CELLVIZIO 100 SERIES AND CELLVIZIO SYSTEMS WITH CONFOCAL MINIPROBES

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    KINGYIELD WRIST BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RIVA STAR SILVER DIAMINE FLUORIDE

    FDA Adverse Event
    Injury ·SDI LIMITED·Product code LBH·February 13, 2019

    AQUILEX FLUID CONTROL SYSTEM

    FDA Adverse Event
    Malfunction ·W.O.M. WORLD OF MEDICINE GMBH·Product code HIG·March 12, 2020

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 19, 2022

    ACCU-CHEK SPIRIT COMBO

    FDA Adverse Event
    Death ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·July 15, 2011

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 10, 2013

    IN TOUCH

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL QUEBEC, LP·Product code FNL·September 16, 2008

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 15, 2023

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·June 28, 2023

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·March 5, 2021